Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency - Wikidata - awgldk - TriplyDB

Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency

Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency

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The "domestication syndrome" in mammals: a unified explanation based on neural crest cell behavior and genetics Ciliopathy Protein Tmem107 Plays Multiple Roles in Craniofacial Development.

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Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency

http://www.wikidata.org/entity/Q33603730

description

2013 nî lūn-bûn

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2013 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի մայիսին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

@zh-hant

2013年論文

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2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

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name

Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency

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Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency

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type

label

Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency

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Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency

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prefLabel

Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency

@ast

Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency

@en

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Cleft Palate: Craniofacial Journal

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Cleft Palate in a Mouse Model of SOX2 Haploinsufficiency

@en

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Kathleen Sulik

http://www.w3.org/2001/XMLSchema#string

Larysa Pevny

http://www.w3.org/2001/XMLSchema#string

Lee Langer

http://www.w3.org/2001/XMLSchema#string

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The cDNA sequence and chromosomal location of the human SOX2 gene

Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome

Expression of Tbx2 and Tbx3 in the developing hypothalamic-pituitary axis

Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans

SOX2 is a dose-dependent regulator of retinal neural progenitor competence

Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes

A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes

SOX2 hypomorphism disrupts development of the prechordal floor and optic cup

Mutations in SOX2 cause anophthalmia.

SOX2, a persistent marker for multipotential neural stem cells derived from embryonic stem cells, the embryo or the adult.

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110-114

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scholarly article

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10.1597/12-260

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1

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51

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2013-05-02T00:00:00Z

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23638914

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haploinsufficiency

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4019342

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